ATE90338T1 - PROCESS FOR THE PREPARATION OF CYPERMETHRIN ISOMERS. - Google Patents

PROCESS FOR THE PREPARATION OF CYPERMETHRIN ISOMERS.

Info

Publication number
ATE90338T1
ATE90338T1 AT90901870T AT90901870T ATE90338T1 AT E90338 T1 ATE90338 T1 AT E90338T1 AT 90901870 T AT90901870 T AT 90901870T AT 90901870 T AT90901870 T AT 90901870T AT E90338 T1 ATE90338 T1 AT E90338T1
Authority
AT
Austria
Prior art keywords
pct
isomer
cypermethrine
isomers
pair
Prior art date
Application number
AT90901870T
Other languages
German (de)
Inventor
Sandor Zoltan
Cyoergy Hidasi
Bela Bertok
Istvan Szekely
Janis Hajimichael
Sandor Botar
Lajos Nagy
Va Somfai
Istvan Lak
Andras Rapi
Antal Gajary
Agnes Hegedues
Maria Tary
Original Assignee
Chinoin Gyogyszer Es Vegyeszet
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from HU16789A external-priority patent/HU199390B/en
Priority claimed from HU678089A external-priority patent/HU210098B/en
Application filed by Chinoin Gyogyszer Es Vegyeszet filed Critical Chinoin Gyogyszer Es Vegyeszet
Application granted granted Critical
Publication of ATE90338T1 publication Critical patent/ATE90338T1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C255/00Carboxylic acid nitriles
    • C07C255/01Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms
    • C07C255/11Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms containing cyano groups and singly-bound oxygen atoms bound to the same saturated acyclic carbon skeleton
    • C07C255/14Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms containing cyano groups and singly-bound oxygen atoms bound to the same saturated acyclic carbon skeleton containing cyano groups and esterified hydroxy groups bound to the carbon skeleton
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N53/00Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Dentistry (AREA)
  • Wood Science & Technology (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Agronomy & Crop Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Pest Control & Pesticides (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Saccharide Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

PCT No. PCT/HU90/00006 Sec. 371 Date Oct. 19, 1990 Sec. 102(e) Date Oct. 19, 1990 PCT Filed Jan. 17, 1990 PCT Pub. No. WO90/08132 PCT Pub. Date Jul. 26, 1990.The invention relates to a process for the preparation of such isomer mixtures of cypermethrine of the Formula (I) <IMAGE> (I) wherein carbon atoms indicated by 1, 3 and alpha stand for a chiral carbon atom and the wavy line indicates cis or trans configuration related to the cyclopropane ring-which contains out of the theoretically possible 8-isomers of cypermethrine at least 95% of 1RtransS and 1StransR (Ib) isomer pair or only a mixture of 1RcisC and 1ScisR (Ia) and the isomer pair (Ib) of the ratio (Ia):(Ib)=55:45-25:75 by asymmetric transformation of second order performed in the presence of an amine base and solvent from a starting cypermethrine isomer mixture which contains next to the isomer pair (Ib) cis and other trans isomers or the isomer pair Ia+Ib at an undesired ratio.
AT90901870T 1989-01-17 1990-01-17 PROCESS FOR THE PREPARATION OF CYPERMETHRIN ISOMERS. ATE90338T1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
HU16789A HU199390B (en) 1989-01-17 1989-01-17 Process for producing mixture of cipermetrin's enantiomeres
HU678089A HU210098B (en) 1989-12-27 1989-12-27 Process for producing isomeric mixtures of cypermethrin and stabilised insecticidal compositions and concentrates containing the mixtures
PCT/HU1990/000006 WO1990008132A1 (en) 1989-01-17 1990-01-17 Process for the preparation of cypermethrine isomers

Publications (1)

Publication Number Publication Date
ATE90338T1 true ATE90338T1 (en) 1993-06-15

Family

ID=26317170

Family Applications (1)

Application Number Title Priority Date Filing Date
AT90901870T ATE90338T1 (en) 1989-01-17 1990-01-17 PROCESS FOR THE PREPARATION OF CYPERMETHRIN ISOMERS.

Country Status (12)

Country Link
US (1) US5153349A (en)
EP (1) EP0404922B1 (en)
KR (1) KR940003358B1 (en)
AT (1) ATE90338T1 (en)
BR (1) BR9004617A (en)
CA (1) CA2020356C (en)
DE (1) DE69001866T2 (en)
DK (1) DK0404922T3 (en)
ES (1) ES2057531T3 (en)
GE (2) GEP19981466B (en)
LV (1) LV10771B (en)
WO (1) WO1990008132A1 (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0601237A1 (en) * 1992-12-09 1994-06-15 Duphar International Research B.V Method of preparing optically active cyanohydrin derivatives
LV12032B (en) * 1995-04-24 1998-09-20 ARGO-CHEMIE Novenyvedoszer Gyarto Ertekesito es Forgalmazo Kft. METHODS OF PESTICIDE COMPOSITIONS AND THEIR ACQUISITION
CN103819363A (en) * 2014-03-21 2014-05-28 中国农科院植保所廊坊农药中试厂 Method of improving transposition synthetic yield of beta-cypermethrin

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4308279A (en) * 1979-06-06 1981-12-29 Fmc Corporation Crystalline, insecticidal pyrethroid
CA1150301A (en) * 1979-11-27 1983-07-19 Michael J. Bull Cyclopropane carboxylic acid ester derivatives
ATE28324T1 (en) * 1982-10-18 1987-08-15 Ici Plc INSECTICIDAL PRODUCT AND ITS MANUFACTURE.
CA1206483A (en) * 1982-11-11 1986-06-24 Johannes Van Berkel Process for preparing cyclopropane carboxylic acid ester derivatives
GB8422872D0 (en) * 1984-09-11 1984-10-17 Ici Plc Insecticidal product
CA1275108A (en) * 1985-01-16 1990-10-09 Laszlo Pap Insecticidal composition comprising more than one active ingredients
DE3522629A1 (en) * 1985-06-25 1987-01-08 Bayer Ag METHOD FOR PRODUCING SPECIFIC ENANTIOMER PAIRS OF PERMETHRINIC ACID (ALPHA) CYANO-3-PHENOXY-4-FLUOR-BENZYL ESTERS
US4997970A (en) * 1987-06-15 1991-03-05 Fmc Corporation Conversion of pyrethroid isomers to move active species
CA1314559C (en) * 1987-06-15 1993-03-16 John Winfrid Ager Conversion of pyrethroid isomers to more active species

Also Published As

Publication number Publication date
BR9004617A (en) 1991-07-30
GEP19981466B (en) 1998-09-25
CA2020356C (en) 2002-09-03
ES2057531T3 (en) 1994-10-16
LV10771A (en) 1995-08-20
DK0404922T3 (en) 1993-07-12
DE69001866D1 (en) 1993-07-15
EP0404922A1 (en) 1991-01-02
US5153349A (en) 1992-10-06
DE69001866T2 (en) 1993-09-23
GEP19981465B (en) 1998-09-25
CA2020356A1 (en) 1990-07-18
WO1990008132A1 (en) 1990-07-26
EP0404922B1 (en) 1993-06-09
LV10771B (en) 1996-06-20
KR910700229A (en) 1991-03-04
KR940003358B1 (en) 1994-04-21

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Legal Events

Date Code Title Description
UEP Publication of translation of european patent specification
EEIH Change in the person of patent owner
REN Ceased due to non-payment of the annual fee